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ANTISEPTIC TOWELETTE by Med-Nap LLC

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 1.1mg in 1.4mL
Labeler: Med-Nap LLC
NDC Code: 59647-750

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Antiseptic Towelette 750

Active Ingredients

Benzalkonium Chloride 0.133%

Purpose

First Aid Antiseptic

Keep out of reach of children.

Caution Keep Out of Reach of Children. If swallowed, get medical help or contact a Poison Control Center right away.

Use

Antiseptic cleansing of face, hands and body without soap and water. Air dries in seconds.

WARNINGS:

For external use only. Do not use in or around the eyes.

Directions

Tear open packet, unfold and use as a washcloth.

Stop Use

if irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse.

Inactive Ingredients

Kathon CG, Water


Antiseptic Towelette Label

WET NAP bulk product Label

MAX

PACKAGING


NDC 59647-750-01

Antiseptic Towelette

Contains Benzalkoniun Chloride

For External use Only

1 Towelette

MAX PACKAGING

Attalla, AL

(256) 538-543www.maxpackaging.com

Made in USA

EXP: 03/2018

LOT MN06916 ABC

WET NAP

60,000

MAX

ANTISEPTIC

LOT #15048 MAX-BZK

ANTISEPTIC  TOWELETTE
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59647-750
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1.1 mg  in 1.4 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
MAGNESIUM CHLORIDE ANHYDROUS 
MAGNESIUM NITRATE 
Packaging
#Item CodePackage Description
1NDC:59647-750-0060000 PACKET in 1 CONTAINER
1NDC:59647-750-011.4 mL in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A02/15/2016
Labeler - Med-Nap LLC (079086400)
Registrant - Med-Nap LLC (079086400)
Establishment
NameAddressID/FEIOperations
Med-Nap LLC079086400manufacture(59647-750)

 
Med-Nap LLC

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Medically reviewed on Feb 9, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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